Involvement of c-myc oncogene in lymphoma cell lines with no detectable chromosome rearrangement of band 8q24

Cancer Genet Cytogenet. 1989 Jul 1;40(1):73-82. doi: 10.1016/0165-4608(89)90147-7.

Abstract

Two lymphoma cell lines of B-cell type were established from Japanese patients with diffuse small noncleaved cell lymphoma. Cytogenetic analysis revealed a 14q+ marker chromosome in both cell lines, and a t(8;14)(q24.1;q32.3) seemed most likely to have occurred. The chromosome 8 pair, however, had no abnormalities. Molecular analysis demonstrated c-myc amplification lacking gross rearrangement in one cell line and genetic rearrangement of c-myc at the first intron as well as aberrant sizes of c-myc mRNA in the other cell line. In the latter case, it is possible that a t(8;14)(q24.1;q32.3) was buried in an unrecognized complex translocation. A combination of cytogenetic and molecular studies to determine the precise nature of the 14q32 translocation is discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Blotting, Northern
  • Blotting, Southern
  • Child, Preschool
  • Chromosome Banding
  • Chromosomes, Human, Pair 14*
  • Chromosomes, Human, Pair 8*
  • DNA Restriction Enzymes
  • Genetic Markers
  • Humans
  • Karyotyping
  • Lymphoma / genetics*
  • Male
  • Proto-Oncogenes*
  • Translocation, Genetic*
  • Tumor Cells, Cultured

Substances

  • Genetic Markers
  • DNA Restriction Enzymes